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Tert-Butyl7-oxo-3-azabicyclo[3.3.1]nonane-3-carboxylate is a bicyclic chemical compound with the molecular formula C13H21NO3. It features a carbonyl group and a tert-butyl group attached to the nitrogen atom within the bicyclic ring, which endows it with unique structural and potential biological properties. Tert-Butyl7-oxo-3-azabicyclo[3.3.1]nonane-3-carboxylate is recognized for its role as a building block in organic synthesis and pharmaceutical research, as well as its potential as a drug candidate for treating various diseases.

909135-31-5

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909135-31-5 Usage

Uses

Used in Pharmaceutical Research:
Tert-Butyl7-oxo-3-azabicyclo[3.3.1]nonane-3-carboxylate is utilized as a key building block in pharmaceutical research for its unique structure, which allows for the development of new drug candidates with potential therapeutic applications in treating a range of diseases.
Used in Organic Synthesis:
In the field of organic synthesis, Tert-Butyl7-oxo-3-azabicyclo[3.3.1]nonane-3-carboxylate serves as an important intermediate, facilitating the creation of complex organic molecules and contributing to the advancement of chemical science.
Used in the Production of Biodegradable Polymers:
Tert-Butyl7-oxo-3-azabicyclo[3.3.1]nonane-3-carboxylate is studied for its potential use in the production of biodegradable polymers, which are environmentally friendly materials that can degrade over time, reducing the impact of plastic waste on the environment.
Used as a Synthetic Intermediate in Organic Chemistry:
Tert-Butyl7-oxo-3-azabicyclo[3.3.1]nonane-3-carboxylate is also recognized for its role as a synthetic intermediate in organic chemistry, where it can be used to synthesize a variety of other organic compounds, expanding the scope of chemical products and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 909135-31-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,9,1,3 and 5 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 909135-31:
(8*9)+(7*0)+(6*9)+(5*1)+(4*3)+(3*5)+(2*3)+(1*1)=165
165 % 10 = 5
So 909135-31-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H21NO3/c1-13(2,3)17-12(16)14-7-9-4-10(8-14)6-11(15)5-9/h9-10H,4-8H2,1-3H3

909135-31-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Azabicyclo[3.3.1]nonane-3-carboxylic acid, 7-oxo-, 1,1-dimethylethyl ester

1.2 Other means of identification

Product number -
Other names tert-Butyl 7-oxo-3-azabicyclo[3.3.1]nonane-3-carboxylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:909135-31-5 SDS

909135-31-5Relevant articles and documents

Structure-activity studies of 7-heteroaryl-3-azabicyclo[3.3.1]non-6-enes: A novel class of highly potent nicotinic receptor ligands

Breining, Scott R.,Melvin, Matt,Bhatti, Balwinder S.,Byrd, Gary D.,Kiser, Melanie N.,Hepler, Christopher D.,Hooker, Dawn N.,Zhang, Jenny,Reynolds, Leslie A.,Benson, Lisa R.,Fedorov, Nikolai B.,Sidach, Serguei S.,Mitchener, J. Pike,Lucero, Linda M.,Lukas, Ronald J.,Whiteaker, Paul,Yohannes, Daniel

, p. 9929 - 9945 (2013/01/16)

The potential for nicotinic ligands with affinity for the α4β2 or α7 subtypes to treat such diverse diseases as nicotine addiction, neuropathic pain, and neurodegenerative and cognitive disorders has been exhibited clinically for several compounds while p

AZABICYCLOALKANE DERIVATIVES USEFUL AS NICOTINIC ACETYLCHOLINE RECEPTOR AGONISTS

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Page/Page column 22, 35, (2010/11/23)

Compounds of the formula I or a pharmaceutically acceptable salt thereof: processes for their preparation, pharmaceutical compositions which contain them and their uses in therapy.

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